Subclinical hyperthyroidism due to a thyrotropin receptor (TSHR) gene mutation (S505R)

Acta Paediatrica, International Journal of Paediatrics

Volumn 95, Issue 12, 2006, Pages 1685-1687

  Pohlenz, Joachim ^a   Pfarr, Nicole ^a   Krüger, Silvia ^b   Hesse, Volker ^c  

^a JOHANNES GUTENBERG UNIVERSITY   (Germany)

^b Children's Hospital Lindenhof ^*  (Germany)

^c SANA KLINIKUM OFFENBACH   (Germany)

Author keywords

Missense mutation; Subclinical hyperthyroidism; Thyrotropin receptor

Indexed keywords

THYROTROPIN RECEPTOR;

ARTICLE; CASE REPORT; CLINICAL FEATURE; CONGENITAL DISORDER; CONGENITAL NON AUTOIMMUNE HYPERTHYROIDISM; DNA SEQUENCE; FEMALE; GENE ACTIVATION; GENE MUTATION; GERM LINE; HETEROZYGOTE; HUMAN; HYPERTHYROIDISM; INFANT; POINT MUTATION; PRIORITY JOURNAL; RECEPTOR GENE; SUBCLINICAL HYPERTHYROIDISM; WEIGHT REDUCTION;

ADULT; FEMALE; HUMANS; HYPERTHYROIDISM; INFANT; MALE; PEDIGREE; POINT MUTATION; RECEPTORS, THYROTROPIN;

EID: 33845249139     PISSN: 08035253     EISSN: 16512227     Source Type: Journal    
DOI: 10.1080/08035250600774122     Document Type: Article

References (11)

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